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Transient ferromagnetic-like state mediating ultrafast reversal of antiferromagnetically coupled spins

机译:类瞬态铁磁态介导反铁磁耦合自旋的超快逆转

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摘要

Ferromagnetic or antiferromagnetic spin ordering is governed by the exchange interaction, the strongest force in magnetism~(1-4). Understanding spin dynamics in magnetic materials is an issue of crucial importance for progress in information processing and recording technology. Usually the dynamics are studied by observing the collective response of exchange-coupled spins, that is, spin resonances, after an external perturbation by a pulse of magnetic field, current or light. The periods of the corresponding resonances range from one nanosecond for ferromagnets down to one picosecond for antiferromagnets. However, virtually nothing is known about the behaviour of spins in a magnetic material after being excited on a timescale faster than that corresponding to the exchange interaction (10-100 fs), that is, in a non-adiabatic way. Here we use the element-specific technique X-ray magnetic circular dichroism to study spin reversal in GdFeCo that is optically excited on a timescale pertinent to the characteristic time of the exchange interaction between Gd and Fe spins. We unexpectedly find that the ultrafast spin reversal in this material, where spins are coupled antiferromagnetically, occurs by way of a transient ferromagnetic-like state. Following the optical excitation, the net magnetizations of the Gd and Fe sublattices rapidly collapse, switch their direction and rebuild their net magnetic moments at substantially different timescales; the net magnetic moment of the Gd sublattice is found to reverse within 1.5 picoseconds, which is substantially slower than the Fe reversal time of 300 femtoseconds. Consequently, a transient state characterized by a temporary parallel alignment of the net Gd and Fe moments emerges, despite their ground-state antiferromagnetic coupling. These surprising observations, supported by atomistic simulations, provide a concept for the possibility of manipulating magnetic order on the timescale of the exchange interaction.
机译:铁磁性或反铁磁性的自旋顺序受交换相互作用的控制,是磁性中最强的力(1-4)。理解磁性材料中的自旋动力学对信息处理和记录技术的进步至关重要。通常,通过在磁场,电流或光的脉冲引起的外部扰动之后,观察交换耦合的自旋的集体响应(即自旋共振)来研究动力学。相应共振的周期范围从铁磁体的1纳秒到反铁磁体的1皮秒。但是,实际上,对于磁性材料中自旋的行为,其时间尺度比对应于交换相互作用的时间(10-100 fs)要快,即以非绝热的方式,实际上一无所知。在这里,我们使用元素特定技术X射线磁性圆二色性来研究GdFeCo中的自旋反转,该自旋反转是在与Gd和Fe自旋之间的交换相互作用的特征时间有关的时间尺度上光学激发的。我们出乎意料地发现,这种材料中的超快自旋反转(自旋反铁磁耦合)是通过类似瞬态铁磁的状态发生的。在光激发之后,Gd和Fe亚晶格的净磁化强度迅速坍塌,切换方向并在实质上不同的时标上重建其净磁矩。发现Gd子晶格的净磁矩在1.5皮秒内反转,这比300毫微秒的Fe反转时间要慢得多。因此,尽管存在基态反铁磁耦合,但仍会出现一个瞬态,其特征是净Gd和Fe矩暂时平行对齐。这些令人惊讶的发现得到原子模拟的支持,为在交换相互作用的时间尺度上操纵磁序的可能性提供了一个概念。

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  • 来源
    《Nature》 |2011年第7342期|p.205-208|共4页
  • 作者单位

    Radboud University Nijmegen,Institute for Molecules and Materials,Heyendaalseweg 135,6525 AJ Nijmegen,The Netherlands,Helmholtz-Zentrum Berlin fur Materialien und Energie, BESSY II, Albert-Einstein-Strasse 15,12489 Berlin, Germany;

    Radboud University Nijmegen,Institute for Molecules and Materials,Heyendaalseweg 135,6525 AJ Nijmegen,The Netherlands;

    Helmholtz-Zentrum Berlin fur Materialien und Energie, BESSY II, Albert-Einstein-Strasse 15,12489 Berlin, Germany;

    Helmholtz-Zentrum Berlin fur Materialien und Energie, BESSY II, Albert-Einstein-Strasse 15,12489 Berlin, Germany;

    Helmholtz-Zentrum Berlin fur Materialien und Energie, BESSY II, Albert-Einstein-Strasse 15,12489 Berlin, Germany;

    Helmholtz-Zentrum Berlin fur Materialien und Energie, BESSY II, Albert-Einstein-Strasse 15,12489 Berlin, Germany,SLAC National Accelerator Laboratory, Menlo Park, California 94025, USA;

    Department of Physics, University of York, York Y0105DD, UK;

    Department of Physics, University of York, York Y0105DD, UK;

    Department of Physics, University of York, York Y0105DD, UK;

    Department of Physics, University of York, York Y0105DD, UK;

    College of Science and Technology, Nihon University, 7-24-1 Funabashi, Chiba, Japan,PRESTO, Japan Science and Technology Agency, 4-1-8 Honcho Kawaguchi,Saitama, Japan;

    College of Science and Technology, Nihon University, 7-24-1 Funabashi, Chiba, Japan;

    Radboud University Nijmegen,Institute for Molecules and Materials,Heyendaalseweg 135,6525 AJ Nijmegen,The Netherlands;

    Radboud University Nijmegen,Institute for Molecules and Materials,Heyendaalseweg 135,6525 AJ Nijmegen,The Netherlands;

    Radboud University Nijmegen,Institute for Molecules and Materials,Heyendaalseweg 135,6525 AJ Nijmegen,The Netherlands;

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